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Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect
Infections with Neisseria meningitidis and Neisseria gonorrhoeae have different clinical manifestations, but the bacteria share up to 80–90% genome sequence identity. The recombinant meningococcal serogroup B (MenB) vaccine 4CMenB consists of four antigenic components that can be present in non-B me...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556335/ https://www.ncbi.nlm.nih.gov/pubmed/34716336 http://dx.doi.org/10.1038/s41541-021-00388-3 |
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author | Ruiz García, Yara Sohn, Woo-Yun Seib, Kate L. Taha, Muhamed-Kheir Vázquez, Julio A. de Lemos, Ana Paula S. Vadivelu, Kumaran Pizza, Mariagrazia Rappuoli, Rino Bekkat-Berkani, Rafik |
author_facet | Ruiz García, Yara Sohn, Woo-Yun Seib, Kate L. Taha, Muhamed-Kheir Vázquez, Julio A. de Lemos, Ana Paula S. Vadivelu, Kumaran Pizza, Mariagrazia Rappuoli, Rino Bekkat-Berkani, Rafik |
author_sort | Ruiz García, Yara |
collection | PubMed |
description | Infections with Neisseria meningitidis and Neisseria gonorrhoeae have different clinical manifestations, but the bacteria share up to 80–90% genome sequence identity. The recombinant meningococcal serogroup B (MenB) vaccine 4CMenB consists of four antigenic components that can be present in non-B meningococcal and gonococcal strains. This comprehensive review summarizes scientific evidence on the genotypic and phenotypic similarities between vaccine antigens and their homologs expressed by non-B meningococcal and gonococcal strains. It also includes immune responses of 4CMenB-vaccinated individuals and effectiveness and impact of 4CMenB against these strains. Varying degrees of strain coverage were estimated depending on the non-B meningococcal serogroup and antigenic repertoire. 4CMenB elicits immune responses against non-B meningococcal serogroups and N. gonorrhoeae. Real-world evidence showed risk reductions of 69% for meningococcal serogroup W clonal complex 11 disease and 40% for gonorrhea after 4CMenB immunization. In conclusion, functional antibody activity and real-world evidence indicate that 4CMenB has the potential to provide some protection beyond MenB disease. |
format | Online Article Text |
id | pubmed-8556335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85563352021-11-15 Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect Ruiz García, Yara Sohn, Woo-Yun Seib, Kate L. Taha, Muhamed-Kheir Vázquez, Julio A. de Lemos, Ana Paula S. Vadivelu, Kumaran Pizza, Mariagrazia Rappuoli, Rino Bekkat-Berkani, Rafik NPJ Vaccines Review Article Infections with Neisseria meningitidis and Neisseria gonorrhoeae have different clinical manifestations, but the bacteria share up to 80–90% genome sequence identity. The recombinant meningococcal serogroup B (MenB) vaccine 4CMenB consists of four antigenic components that can be present in non-B meningococcal and gonococcal strains. This comprehensive review summarizes scientific evidence on the genotypic and phenotypic similarities between vaccine antigens and their homologs expressed by non-B meningococcal and gonococcal strains. It also includes immune responses of 4CMenB-vaccinated individuals and effectiveness and impact of 4CMenB against these strains. Varying degrees of strain coverage were estimated depending on the non-B meningococcal serogroup and antigenic repertoire. 4CMenB elicits immune responses against non-B meningococcal serogroups and N. gonorrhoeae. Real-world evidence showed risk reductions of 69% for meningococcal serogroup W clonal complex 11 disease and 40% for gonorrhea after 4CMenB immunization. In conclusion, functional antibody activity and real-world evidence indicate that 4CMenB has the potential to provide some protection beyond MenB disease. Nature Publishing Group UK 2021-10-29 /pmc/articles/PMC8556335/ /pubmed/34716336 http://dx.doi.org/10.1038/s41541-021-00388-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Ruiz García, Yara Sohn, Woo-Yun Seib, Kate L. Taha, Muhamed-Kheir Vázquez, Julio A. de Lemos, Ana Paula S. Vadivelu, Kumaran Pizza, Mariagrazia Rappuoli, Rino Bekkat-Berkani, Rafik Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title | Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title_full | Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title_fullStr | Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title_full_unstemmed | Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title_short | Looking beyond meningococcal B with the 4CMenB vaccine: the Neisseria effect |
title_sort | looking beyond meningococcal b with the 4cmenb vaccine: the neisseria effect |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556335/ https://www.ncbi.nlm.nih.gov/pubmed/34716336 http://dx.doi.org/10.1038/s41541-021-00388-3 |
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